US11276900B2 - Nonaqueous electrolyte secondary battery and method of producing the same - Google Patents

Nonaqueous electrolyte secondary battery and method of producing the same Download PDF

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US11276900B2
US11276900B2 US15/782,241 US201715782241A US11276900B2 US 11276900 B2 US11276900 B2 US 11276900B2 US 201715782241 A US201715782241 A US 201715782241A US 11276900 B2 US11276900 B2 US 11276900B2
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negative electrode
sheet
nonaqueous electrolyte
filling layer
secondary battery
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US20180114970A1 (en
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Shinsuke MATSUHARA
Kazuhisa Takeda
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Toyota Motor Corp
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    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/40—Separators; Membranes; Diaphragms; Spacing elements inside cells
    • H01M50/409—Separators, membranes or diaphragms characterised by the material
    • H01M50/449—Separators, membranes or diaphragms characterised by the material having a layered structure
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
    • H01M4/621—Binders
    • H01M4/622—Binders being polymers
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D127/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers
    • C09D127/02—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment
    • C09D127/12—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
    • C09D127/16—Homopolymers or copolymers of vinylidene fluoride
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/04—Construction or manufacture in general
    • H01M10/0431—Cells with wound or folded electrodes
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/056—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes
    • H01M10/0564—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes the electrolyte being constituted of organic materials only
    • H01M10/0565—Polymeric materials, e.g. gel-type or solid-type
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/056—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes
    • H01M10/0564—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes the electrolyte being constituted of organic materials only
    • H01M10/0566—Liquid materials
    • H01M10/0567—Liquid materials characterised by the additives
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/058—Construction or manufacture
    • H01M10/0587—Construction or manufacture of accumulators having only wound construction elements, i.e. wound positive electrodes, wound negative electrodes and wound separators
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/40—Separators; Membranes; Diaphragms; Spacing elements inside cells
    • H01M50/409—Separators, membranes or diaphragms characterised by the material
    • H01M50/449—Separators, membranes or diaphragms characterised by the material having a layered structure
    • H01M50/451—Separators, membranes or diaphragms characterised by the material having a layered structure comprising layers of only organic material and layers containing inorganic material
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/40—Separators; Membranes; Diaphragms; Spacing elements inside cells
    • H01M50/46—Separators, membranes or diaphragms characterised by their combination with electrodes
    • H01M50/461—Separators, membranes or diaphragms characterised by their combination with electrodes with adhesive layers between electrodes and separators
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/50—Current conducting connections for cells or batteries
    • H01M50/531—Electrode connections inside a battery casing
    • H01M50/538—Connection of several leads or tabs of wound or folded electrode stacks
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
    • C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
    • C08G65/04—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers only
    • C08G65/06—Cyclic ethers having no atoms other than carbon and hydrogen outside the ring
    • C08G65/08—Saturated oxiranes
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M2300/00—Electrolytes
    • H01M2300/0085—Immobilising or gelification of electrolyte
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10—Energy storage using batteries
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
    • Y02P70/50—Manufacturing or production processes characterised by the final manufactured product

Definitions

  • the present disclosure relates to a nonaqueous electrolyte secondary battery and a method of producing the same, and specifically, to a nonaqueous electrolyte secondary battery including a flat wound electrode body and a method of producing the same.
  • a flat wound electrode body is accommodated in a battery case together with a nonaqueous electrolyte.
  • the flat wound electrode body is produced such that, for example, a band-like positive electrode sheet including a positive electrode active material layer and a band-like negative electrode sheet including a negative electrode active material layer are wound with a band-like separator sheet therebetween, and are additionally pressed and bent to be flat (refer to Japanese Patent Application Publication No. 2010-287513 (JP 2010-287513 A)).
  • a nonaqueous electrolyte secondary battery including a flat wound electrode body substances derived from charge carriers (for example, Li) are likely to precipitate locally on a negative electrode.
  • charge carriers for example, Li
  • relatively large stress is applied to a portion (wound R portion) that is greatly bent when the flat wound electrode body is produced compared to a portion (flat wound portion) that is less deformed.
  • wrinkles are generated in a separator at a boundary portion between the wound R portion and the flat wound portion, and a large gap may be formed locally between the negative electrode and the separator.
  • a portion with a large gap a distance between positive and negative electrodes increases, and electrical resistance becomes relatively higher.
  • reception of charge carriers in the negative electrode is not sufficient, and substances derived from charge carriers may precipitate on the negative electrode.
  • the present disclosure provides a nonaqueous electrolyte secondary battery which includes a flat wound electrode body and in which precipitation of substances derived from charge carriers on a negative electrode is prevented.
  • a nonaqueous electrolyte secondary battery including a flat wound electrode body that includes a positive electrode sheet, a negative electrode sheet, and a separator sheet arranged between the positive electrode sheet and the negative electrode sheet, and a nonaqueous electrolyte, wherein the wound electrode body includes a filling layer containing a thermal polymerization product of a resin having electrolyte solution swellability between the negative electrode sheet and the separator sheet.
  • the filling layer fills a gap between the negative electrode and the separator, and thus it is possible to reduce a difference in distance between positive and negative electrodes. Accordingly, a charging and discharging reaction can be relatively uniformized compared to a battery without the filling layer. As a result, it is possible to appropriately prevent precipitation of substances derived from charge carriers on the negative electrode.
  • the filling layer may be formed integrally with at least one of the negative electrode sheet and the separator sheet. Thereby, it is possible to reduce a difference in a distance between positive and negative electrodes more appropriately, and it is possible to increase precipitation resistance with respect to substances derived from charge carriers to a higher degree.
  • the filling layer may be formed integrally with the negative electrode sheet.
  • the filling layer may be formed integrally with the separator sheet.
  • the filling layer that is in a state of being independent of the negative electrode sheet and the separator sheet may be arranged between the negative electrode sheet and the separator sheet.
  • the nonaqueous electrolyte may include a polymerization agent used when a resin included in the filling layer is thermally polymerized, for example, at least one of a polymerization initiator, a chain transfer agent, and a polymerization terminator.
  • a polymerization agent used when a resin included in the filling layer is thermally polymerized for example, at least one of a polymerization initiator, a chain transfer agent, and a polymerization terminator.
  • a weight average molecular weight of the thermal polymerization product of the resin having electrolyte solution swellability may be 10,000 to 1,000,000.
  • a weight per unit area of the filling layer may be 0.2 mg/cm 2 or more.
  • the resin having electrolyte solution swellability may be polyethylene oxide.
  • a method of producing a nonaqueous electrolyte secondary battery including, preparing a flat wound electrode body that includes a positive electrode sheet, a negative electrode sheet, and a separator sheet arranged between the positive electrode sheet and the negative electrode sheet; accommodating the wound electrode body in which a filling layer including a resin having electrolyte solution swellability is interposed between the negative electrode sheet and the separator sheet and a nonaqueous electrolyte in a battery case to produce an assembly; and warming the assembly in which the nonaqueous electrolyte includes at least one of a polymerization initiator, a chain transfer agent, and a polymerization terminator and thermally polymerizing the resin included in the filling layer.
  • FIG. 1 is a cross-sectional view schematically showing an internal structure of a nonaqueous electrolyte secondary battery according to an embodiment
  • FIG. 2 is a schematic diagram showing a configuration of the wound electrode body of FIG. 1 ;
  • FIG. 3 is a schematic diagram showing a partial cross-sectional structure of the wound electrode body of FIG. 1 ;
  • FIG. 4 is a flowchart showing a production method according to an embodiment
  • FIG. 5 is a schematic diagram showing a partial cross-sectional structure of a wound electrode body according to another embodiment.
  • FIG. 6 is a schematic diagram showing a partial cross-sectional structure of a wound electrode body according to another embodiment.
  • FIG. 1 is a cross-sectional view schematically showing an internal structure of a nonaqueous electrolyte secondary battery according to an embodiment.
  • a nonaqueous electrolyte secondary battery 100 shown in FIG. 1 has a configuration in which a wound electrode body 40 and a nonaqueous electrolyte (not shown) are accommodated in a battery case 50 .
  • the battery case 50 includes a rectangular parallelepiped (rectangular) battery case body 52 having an upper end that is open and a bottom and a cover plate 54 for closing the opening.
  • a positive electrode terminal 70 and a negative electrode terminal 72 for external connection are provided in the cover plate 54 .
  • FIG. 2 is a schematic diagram showing a configuration of the wound electrode body 40 .
  • FIG. 3 is a schematic diagram showing a partial cross-sectional structure of the wound electrode body 40 .
  • the wound electrode body 40 includes a band-like positive electrode sheet 10 , a band-like negative electrode sheet 20 , and a band-like separator sheet 30 .
  • a filling layer 26 is arranged on a surface of the negative electrode sheet 20 .
  • the wound electrode body 40 is formed by laminating the positive electrode sheet 10 and the negative electrode sheet 20 including the filling layer 26 with the separator sheet 30 therebetween and winding them in a longitudinal direction.
  • An appearance of the wound electrode body 40 has a flat shape.
  • the wound electrode body 40 has a substantially rounded rectangular shape in a cross section orthogonal to a winding axis.
  • the positive electrode sheet 10 includes a band-like positive electrode current collector 12 and a positive electrode active material layer 14 formed on a surface thereof.
  • a conductive member made of a metal having favorable conductivity for example, aluminum and nickel
  • the positive electrode active material layer 14 is formed with a predetermined width on a surface of the positive electrode current collector 12 in the longitudinal direction. At one end (the left side in FIG. 1 and FIG. 2 ) of the positive electrode current collector 12 in a width direction, a positive electrode active material layer non-forming portion 12 n in which the positive electrode active material layer 14 is not formed is provided.
  • the positive electrode sheet 10 is electrically connected to the positive electrode terminal 70 through a positive electrode current collector plate 12 c provided in the positive electrode active material layer non-forming portion 12 n.
  • the positive electrode active material layer 14 includes a positive electrode active material.
  • the positive electrode active material lithium transition metal composite oxides, for example, LiNiO 2 , LiCoO 2 , LiMn 2 O 4 , LiNi 1/3 Co 1/3 Mn 1/3 O 2 , and LiNi 0.5 Mn 1.5 O 4 , are preferable.
  • the positive electrode active material layer 14 may include components other than the positive electrode active material, for example, a conductive material and a binder.
  • the conductive material carbon materials, for example, carbon black (for example, acetylene black and Ketjenblack), activated carbon, and graphite, are exemplified.
  • the binder for example, a halogenated vinyl resin such as polyvinylidene fluoride (PVdF) and a polyalkylene oxide such as polyethylene oxide (PEO) are exemplified.
  • the negative electrode sheet 20 includes a band-like negative electrode current collector 22 and a negative electrode active material layer 24 formed on a surface thereof.
  • a conductive member made of a metal having favorable conductivity for example, copper and nickel
  • the negative electrode active material layer 24 is formed with a predetermined width on a surface of the negative electrode current collector 22 in the longitudinal direction. At one end (right side in FIG. 1 and FIG. 2 ) of the negative electrode current collector 22 in the width direction, a negative electrode active material layer non-forming portion 22 n in which the negative electrode active material layer 24 is not formed is provided.
  • the negative electrode sheet 20 is electrically connected to the negative electrode terminal 72 through a negative electrode current collector plate 22 c provided in the negative electrode active material layer non-forming portion 22 n.
  • the negative electrode active material layer 24 includes a negative electrode active material.
  • a graphite carbon material such as natural graphite, artificial graphite, and amorphous coated graphite (in a form in which amorphous carbon is applied to surfaces of graphite particles) is preferable.
  • the negative electrode active material layer 24 may include components other than the negative electrode active material, for example, a thickener and a binder.
  • a thickener for example, celluloses such as carboxymethyl cellulose (CMC) and methylcellulose (MC) are exemplified.
  • the binder for example, rubbers such as styrene butadiene rubber (SBR) and a halogenated vinyl resin such as polyvinylidene fluoride (PVdF) are exemplified.
  • the negative electrode sheet 20 of the present embodiment includes the filling layer 26 on a surface on the side that does not face the negative electrode current collector 22 of the negative electrode active material layer 24 .
  • the filling layer 26 is physically adhered to and integrated with the negative electrode active material layer 24 of the negative electrode sheet 20 .
  • the filling layer 26 is provided on the negative electrode sheet 20 , it is possible to prevent precipitation of substances derived from charge carriers on the negative electrode sheet 20 more appropriately. Therefore, the effect of the technology disclosed herein can be exhibited to a high degree.
  • the filling layer 26 includes a thermal polymerization product of a resin having electrolyte solution swellability.
  • resin having electrolyte solution swellability in this specification refers to a resin having a swelling ratio with respect to an electrolyte solution of 110% or more, preferably 113% or more, for example, 110 to 200%.
  • the swelling ratio of the resin can be obtained by the following method. That is, first, a resin material is dissolved in a predetermined solvent (for example, acetonitrile) and poured into a Petri dish made of Teflon (registered trademark). Next, the result is placed in a reduced pressure dryer and dried to obtain a sample with a thickness of about 100 ⁇ m.
  • a predetermined solvent for example, acetonitrile
  • the obtained sample is cut into predetermined areas, and an average thickness (thickness A) is measured accurately. Then, a volume (volume A) of the sample is calculated based on area ⁇ thickness A. Next, this sample is immersed in a predetermined electrolyte solution and left at a temperature of 25° C. for 5 days. After 5 days, the sample is removed from the electrolyte solution, and an average thickness (thickness B) is measured. Next, a volume (volume B) of the sample after immersion in the electrolyte solution is calculated based on area ⁇ thickness B. Then, the volume B is divided by the volume A to calculate a “swelling ratio of a resin with respect to an electrolyte solution” converted to a percentage.
  • a polyether resin such as polyethylene oxide (PEO), polypropylene oxide (PPO), tetrafluoroethylene-perfluoroalkyl vinyl ether copolymer (PFA), polyoxyethylene alkyl ether (AE), polyoxyethylene alkyl phenyl ether (APE), polyethylene glycol (PEG), and polypropylene glycol (PPG), and an acrylic resin such as polymethylmethacrylate (PMMA), poly(meth)acrylic acid (here, (meth)acrylic acid means that acrylic acid and methacrylic acid are included), polyacrylonitrile (PAN), and polyvinyl alcohol (PVA) are exemplified.
  • PEO polyethylene oxide
  • PPO polypropylene oxide
  • PFA tetrafluoroethylene-perfluoroalkyl vinyl ether copolymer
  • AE polyoxyethylene alkyl ether
  • APE polyoxyethylene alkyl phenyl ether
  • PEG polyethylene glycol
  • PPG poly
  • the above resin is thermally polymerized and crosslinked. Thereby, a network between resin members is strengthened.
  • the compatibility between the filling layer 26 and a nonaqueous electrolyte becomes strong and it is possible to enhance an electrolyte solution holding property of the filling layer 26 .
  • a swelling ratio with respect to an electrolyte solution can be increased by 5% or more, and typically 5 to 20%, for example, about 10 ⁇ 5%, compared to a resin before thermal polymerization and crosslinking.
  • the filling layer 26 can function as a cushioning material and a distance between positive and negative electrodes can be appropriately uniformized.
  • determination of whether the above resin is thermally polymerized can be performed by, for example, the following method. That is, first, a battery is disassembled, and a sample with a predetermined size is cut out from a member including the filling layer 26 . Next, the weight of the filling layer 26 is measured and it is then left at a temperature of 25° C. for 6 hours under an inert or atmospheric atmosphere. After 6 hours, the weight of the filling layer 26 is measured again. Then, the weight obtained after being left for 6 hours is divided by the weight before being left to calculate a “weight change ratio” converted to a percentage. When the weight change ratio is approximately 5% or less, and preferably 3% or less, it can be determined that “the resin of the filling layer 26 is thermally polymerized and crosslinked.”
  • the thermal polymerization product of the above resin may have a structure derived from a polymerization agent used for thermal polymerization, for example, a polymerization agent such as a polymerization initiator, a chain transfer agent, and a polymerization terminator at a main chain terminal.
  • a polymerization agent such as a polymerization initiator, a chain transfer agent, and a polymerization terminator at a main chain terminal.
  • a cationic group such as an amino group derived from a polymerization agent included in a nonaqueous electrolyte of the nonaqueous electrolyte secondary battery 100 and an anionic group such as a carboxy group, a hydroxy group, a sulfo group, a sulfate group, a phosphate group, and a phosphonic acid group may be included at a main chain terminal.
  • a weight average molecular weight (an average molecular weight based on the weight measured by Gel Permeation Chromatography (GPC) using a standard substance) of the thermal polymerization product of the above resin is not particularly limited, and may be approximately 1000 or more, preferably 10,000 or more, for example, about 10,000 to 1,000,000. Thereby, it is possible to further enhance an electrolyte solution holding property in the filling layer 26 and the effect of the technology disclosed herein can be stably exhibited to a higher degree.
  • a weight per unit area of the filling layer 26 is not particularly limited, and may be approximately 0.01 mg/cm 2 or more, and typically 0.1 mg/cm 2 or more, for example, 0.2 mg/cm 2 or more. Thereby, the effect of the technology disclosed herein can be exhibited to a higher degree.
  • An upper limit value of the weight per unit area is not particularly limited, and typically, it is smaller than a weight per unit area of the positive electrode active material layer 14 or the negative electrode active material layer 24 and may be approximately 10 mg/cm 2 or less, for example, 5 mg/cm 2 or less.
  • the thickness of the filling layer 26 is not particularly limited, and it is typically thinner than the thickness of the positive electrode active material layer 14 of the positive electrode sheet 10 or the negative electrode active material layer 24 of the negative electrode sheet 20 .
  • the thickness of the filling layer 26 may be thinner than the thickness of a resin base material 32 or a heat resistant layer 34 of the separator sheet 30 .
  • the thickness of the filling layer 26 may be, for example, approximately 0.01 ⁇ m or more, for example, 0.05 ⁇ m or more, and approximately 5 ⁇ m or less, for example, 1 ⁇ m or less.
  • the separator sheet 30 is arranged between the positive electrode sheet 10 and the filling layer 26 on the negative electrode sheet 20 .
  • the separator sheet 30 insulates the positive electrode active material layer 14 and the negative electrode active material layer 24 .
  • the separator sheet 30 is porous so that charge carriers included in a nonaqueous electrolyte can pass therethrough.
  • the separator sheet 30 stores a nonaqueous electrolyte in pores, and forms an ion conduction path between the positive electrode active material layer 14 and the negative electrode active material layer 24 .
  • the separator sheet 30 includes the band-like resin base material 32 and the heat resistant layer (HRL layer) 34 formed on a surface thereof. However, the separator sheet 30 may not include the heat resistant layer 34 . In the present embodiment, the heat resistant layer 34 is arranged to face the negative electrode sheet 20 . However, the heat resistant layer 34 may be arranged to face the positive electrode sheet 10 .
  • the resin base material 32 for example, a porous resin sheet (film) made of a polyolefin resin such as polyethylene (PE) and polypropylene (PP), a polyvinyl chloride resin, a polyvinyl acetate resin, a polyimide resin, a polyamide resin, and celluloses and the like are exemplified.
  • the heat resistant layer 34 includes inorganic compound particles (inorganic filler) such as alumina.
  • the heat resistant layer 34 has heat resistance and an insulation property. When the heat resistant layer 34 is provided, for example, even if the temperature inside the nonaqueous electrolyte secondary battery 100 exceeds a melting point of a resin included in the resin base material 32 and the resin base material 32 shrinks and breaks, it is possible to prevent short circuiting between the positive electrode sheet 10 and the negative electrode sheet 20 .
  • the thickness of the resin base material 32 is not particularly limited, and may be approximately 5 ⁇ m or more, for example, 10 ⁇ m or more, and approximately 50 ⁇ m or less, preferably 30 ⁇ m or less, for example, 25 ⁇ m or less.
  • the thickness of the heat resistant layer 34 is not particularly limited, and may be approximately 0.5 ⁇ m or more, for example, 1 ⁇ m or more, and approximately 20 ⁇ m or less, preferably 10 ⁇ m or less, for example, 5 ⁇ m or less.
  • the nonaqueous electrolyte typically includes a nonaqueous solvent and a supporting salt.
  • the nonaqueous electrolyte is typically in a liquid state in a temperature range (for example, in a range of ⁇ 10° C. to +50° C.) in which the nonaqueous electrolyte secondary battery 100 is generally used.
  • the nonaqueous solvent for example, nonaqueous solvents such as carbonates, esters, ethers, nitriles, sulfones, and lactones are exemplified. Among them, carbonates such as ethylene carbonate (EC), diethyl carbonate (DEC), dimethyl carbonate (DMC), and ethyl methyl carbonate (EMC) are preferable.
  • the supporting salt dissociates in a nonaqueous solvent and charge carriers are generated.
  • a lithium salt, a sodium salt, a magnesium salt, and the like are exemplified.
  • a lithium salt such as LiPF 6 or LiBF 4 is preferable.
  • a polymerization agent that is used when the resin of the filling layer 26 is thermally polymerized and crosslinked for example, a polymerization initiator, a chain transfer agent (also referred to as a molecular weight regulator or a polymerization degree regulator), a polymerization terminator, and the like may remain in the nonaqueous electrolyte.
  • organic peroxides such as peroxyesters, peroxidic carbonates, diacyl peroxides, dialkyl peroxides, hydroperoxides, and peroxy ketals are exemplified.
  • t-butyl peroxypivalate t-hexyl peroxypivalate, t-butyl peroxy-2-ethylhexanoate, t-butyl peroxypropylcarbonate, t-butyl peroxylaurate, t-butyl peroxybenzoate, isobutyryl peroxide, lauroyl peroxide, benzoyl peroxide, dipropyl peroxydicarbonate, diisopropyl peroxydicarbonate, t-butyl hydroperoxide, 1,1-bis(t-butylperoxy)-2-methylcyclohexane, 1,1-bis(t-butylperoxy)cyclohexane, 1,1-bis(t-butylperoxy)-3,3,5-trimethylcyclohexane, and the like are exemplified.
  • azo compounds such as 2,2′-azobisisobutyronitrile, 2,2′-azobis(2-amidinopropane)dihydrochloride, 2,2′-azobis(2,4-dimethylvaleronitrile), 2,2′-azobis(2-methylbutyronitrile), 1,1′-azobis (cyclohexane-1-carbonitrile), 2,2′-azobis(2,4,4-trimethylpentane), and dimethyl 2,2′-azobis(2-methylpropionate) are exemplified.
  • a carboxylic acid having no hydroxy group such as caproic acid, lauric acid, stearic acid, and methoxyacetic acid
  • a hydroxy acid such as hydroxylamine sulfonic acid, hydroxydimethylbenzenethiocarboxylic acid, and hydroxydibutylbenzenethiocarboxylic acid
  • the nonaqueous electrolyte may include, for example, a gas generating agent such as biphenyl (BP) and cyclohexylbenzene (CHB), a film forming agent such as an oxalato complex compound containing boron atoms and/or phosphorus atoms and vinylene carbonate (VC), various additives such as a dispersant and a thickener, and the like.
  • a gas generating agent such as biphenyl (BP) and cyclohexylbenzene (CHB)
  • a film forming agent such as an oxalato complex compound containing boron atoms and/or phosphorus atoms and vinylene carbonate (VC)
  • various additives such as a dispersant and a thickener, and the like.
  • the nonaqueous electrolyte secondary battery 100 can be produced according to procedures shown in FIG. 4 .
  • a production method shown in FIG. 4 includes a process of preparing a wound electrode body (Step S 1 ), a process of producing an assembly (Step S 2 ), and a process of thermally polymerizing a resin (Step S 3 ).
  • a general process of producing a battery may be the same as in the related art.
  • a flat wound electrode body including a precursor of the filling layer 26 is prepared.
  • the positive electrode sheet 10 including the positive electrode current collector 12 and the positive electrode active material layer 14 is prepared.
  • the negative electrode sheet 20 which includes the negative electrode current collector 22 and the negative electrode active material layer 24 and is integrated with the precursor of the filling layer 26 is prepared.
  • the separator sheet 30 including the resin base material 32 and the heat resistant layer 34 is prepared.
  • the positive electrode sheet 10 can be produced by preparing a positive electrode paste containing a positive electrode active material, applying it to a surface of the band-like positive electrode current collector 12 , and drying it.
  • the negative electrode sheet 20 can be produced by preparing a negative electrode paste containing a negative electrode active material, applying it to a surface of the band-like negative electrode current collector 22 , and drying it.
  • the precursor of the filling layer 26 on the negative electrode sheet 20 can be produced by preparing a paste containing a resin having electrolyte solution swellability, applying it to a surface of the negative electrode active material layer 24 , and drying it.
  • the separator sheet 30 can be produced by preparing a paste containing an inorganic filler, applying it to a surface of the band-like resin base material 32 , and drying it.
  • the positive electrode sheet 10 and the negative electrode sheet 20 including the precursor of the filling layer 26 are laminated with the separator sheet 30 therebetween and wound in the longitudinal direction to produce a cylindrical wound electrode body.
  • the precursor of the filling layer 26 faces the separator sheet 30 .
  • the precursor of the filling layer 26 is interposed between the negative electrode sheet 20 and the separator sheet 30 .
  • the cylindrical wound electrode body is pressed and bent to be flat. Thereby, the flat wound electrode body can be produced.
  • Step S 2 In the process of producing an assembly, the wound electrode body obtained in Step S 1 is accommodated in the battery case 50 together with a nonaqueous electrolyte.
  • the nonaqueous electrolyte includes a polymerization agent used when a resin included in the precursor of the filling layer 26 is thermally polymerized, for example, a polymerization initiator, a chain transfer agent, a polymerization terminator, or the like.
  • the polymerization agent can be appropriately selected from among known agents described above or conventional agents.
  • An amount of polymerization agent used may be an amount that is generally used.
  • An amount of polymerization agent used may be, for example, approximately 0.005 to 1 parts by mass, for example, about 0.01 to 1 parts by mass, with respect to 100 parts by mass of a resin component included in the precursor of the filling layer 26 and also may be approximately 0.001 to 5 mass %, typically 0.01 to 3 mass %, for example, about 1 to 3 mass %, when there is 100 mass % of the nonaqueous electrolyte in total.
  • the assembly may be unsealed or sealed. When the assembly is sealed, it is possible to enhance a handling property and workability when the resin is thermally polymerized in the following step.
  • Step S 3 In the process of thermally polymerizing a resin, the assembly obtained in Step S 2 is warmed, and the resin included in the precursor of the filling layer 26 is thermally polymerized.
  • the assembly is aged under a temperature environment at 40° C. or higher for a predetermined time.
  • the aging conditions for example, a temperature and a time, can be appropriately set according to the type of a resin, a type of a polymerization agent used, and the like.
  • the aging temperature is not particularly limited, and may be typically 40 to 80° C., for example, about 60 to 80° C.
  • the aging time can be set based on, for example, the aging temperature, and a 1 hour half-life temperature of the polymerization agent. Thereby, it is possible to produce the nonaqueous electrolyte secondary battery 100 including the filling layer 26 containing a thermal polymerization product of a resin having electrolyte solution swellability between the negative electrode sheet 20 and the separator sheet 30 .
  • the filling layer 26 is provided on the negative electrode sheet 20 in the present embodiment, but the present disclosure is not limited thereto.
  • the filling layer disclosed herein may be arranged between the negative electrode sheet and the separator sheet.
  • the filling layer may be provided on, for example, the separator sheet.
  • a filling layer that is in a state of being independent of the negative electrode sheet and the separator sheet may be arranged between the negative electrode sheet and the separator sheet.
  • FIG. 5 is a schematic diagram showing a partial cross-sectional structure of a wound electrode body 40 A according to a second embodiment.
  • the wound electrode body 40 A of the second embodiment includes a positive electrode sheet 10 , a negative electrode sheet 20 A, and a separator sheet 30 A.
  • the positive electrode sheet 10 is the same as in the first embodiment.
  • the negative electrode sheet 20 A includes the negative electrode current collector 22 and the negative electrode active material layer 24 .
  • no filling layer is provided on the negative electrode sheet 20 A.
  • the separator sheet 30 A includes the resin base material 32 and the heat resistant layer 34 .
  • the separator sheet 30 A includes a filling layer 36 on a surface on the side that does not face the resin base material 32 of the heat resistant layer 34 . In other words, the filling layer 36 is physically adhered to and integrated with the heat resistant layer 34 of the separator sheet 30 A.
  • the filling layer 36 is arranged on the side that faces the negative electrode sheet 20 A.
  • FIG. 6 is a schematic diagram showing a partial cross-sectional structure of a wound electrode body 40 B according to a third embodiment.
  • the wound electrode body 40 B of the third embodiment includes a positive electrode sheet 10 , a negative electrode sheet 20 B, a separator sheet 30 B and a filling sheet 38 .
  • the positive electrode sheet 10 is the same as in the first embodiment.
  • the negative electrode sheet 20 B includes the negative electrode current collector 22 and the negative electrode active material layer 24 . Unlike the first embodiment, no filling layer is provided on the negative electrode sheet 20 B.
  • the separator sheet 30 B is the same as in the first embodiment.
  • the filling sheet 38 that is in a state of being independent of the negative electrode sheet 20 B and the separator sheet 30 B may be arranged between the negative electrode sheet 20 B and the separator sheet 30 B.
  • the nonaqueous electrolyte secondary battery 100 can be used for various applications, and when the wound electrode body 40 is included, a high energy density and a high capacity can be realized.
  • precipitation resistance for example, Li precipitation resistance
  • it can be appropriately used as, for example, a power source (drive power supply) of a hybrid vehicle or an electric vehicle using such characteristics.
  • ⁇ Production of a battery of Comparative Example 1> LiNi 1/3 Co 1/3 Mn 1/3 O 2 (NCM, average particle size of 5 ⁇ m) as a positive electrode active material, polyvinylidene fluoride (PVdF) as a binder, and acetylene black (AB) as a conductive material were weighed out such that the mass ratio (solid content ratio) was NCM:PVdF:AB 92:3:5, and mixed into N-methyl-2-pyrrolidone (NMP) to prepare a positive electrode paste.
  • the positive electrode paste was applied to a band-like aluminum foil with a thickness of 15 ⁇ m, dried, and pressed to a predetermined thickness to produce a positive electrode sheet including a positive electrode active material layer with a width of 100 mm.
  • the negative electrode paste was applied to a band-like copper foil with a thickness of 10 ⁇ m, dried and then pressed to a predetermined thickness to produce a negative electrode sheet including a negative electrode active material layer with a width of 105 mm.
  • a porous sheet including a heat resistant layer (HRL layer, thickness of 4 ⁇ m) containing a ceramic on a surface of a resin base material (total thickness of 24 ⁇ m) having a 3-layer (PP/PE/PP) structure in which a polypropylene layer (PP layer) was laminated on both sides of a polyethylene layer (PE layer) was prepared.
  • the above positive electrode sheet and negative electrode sheet were laminated with the separator sheet therebetween, wound, and additionally pressed and bent to be flat to produce a flat wound electrode body.
  • the positive electrode current collector plate was welded to the positive electrode sheet of the wound electrode body, the negative electrode current collector plate was welded to the negative electrode sheet thereof, and these were enclosed in a battery case together with the nonaqueous electrolyte. Thereby, the assembly was obtained.
  • the assembly was left for a predetermined time, and the nonaqueous electrolyte solution was impregnated into the wound electrode body. Then, charging was performed to a predetermined voltage, and aging was performed at 60° C. in the charged state.
  • the battery of Comparative Example 1 was produced.
  • a porous sheet made of polyethylene (PE, swelling ratio with respect to an electrolyte solution: 101%) was prepared. Then, a battery of Comparative Example 2 was produced in the same manner as in Comparative Example 1 except that the PE porous sheet was interposed between the separator sheet and the negative electrode sheet when the above wound electrode body was produced.
  • a porous sheet made of polypropylene (PP, swelling ratio with respect to an electrolyte solution: 105%) was prepared. Then, a battery of Comparative Example 3 was produced in the same manner as in Comparative Example 1 except that the PP porous sheet was interposed between the separator sheet and the negative electrode sheet when the above wound electrode body was produced.
  • a porous sheet made of polyethylene oxide (PEO, swelling ratio with respect to an electrolyte solution: 123%) was prepared. Then, a battery of Comparative Example 4 was produced in the same manner as in Comparative Example 1 except that the PEO porous sheet was interposed between the separator sheet and the negative electrode sheet when the above wound electrode body was produced.
  • Example 1 ⁇ Production of a battery of Example 1> A battery of Example 1 was produced in the same manner as in Comparative Example 4 except that ⁇ -methyl styrene dimer as a chain transfer agent and t-hexyl peroxypivalate (PERHEXYL (registered trademark) PV) as a polymerization initiator were additionally added at 1.1 mass % and 1.9 mass % as a percentage, respectively, to the nonaqueous electrolyte.
  • the wound electrode body of the battery of Example 1 has a configuration shown in FIG. 6 .
  • a polyethylene oxide layer (PEO layer) was formed on a surface of a negative electrode active material layer of a negative electrode sheet instead of using a PEO sheet.
  • polyethylene oxide powder was dissolved in acetonitrile to prepare a slurry having a solid fraction of 60%. This slurry was applied to the surface of the negative electrode active material layer by a spray dry method to form a PEO layer (weight per unit area of 0.5 mg/cm 2 ).
  • a battery of Example 2 was produced in the same manner as in Example 1 except that a negative electrode including the PEO layer was used in place of the PEO sheet and the negative electrode sheet.
  • a wound electrode body of the battery of Example 2 had a configuration shown in FIG. 3 .
  • a PEO layer was formed on a surface of an HRL layer of a separator sheet without using a PEO sheet. Specifically, in the same manner as in Example 2, the PEO layer (weight per unit area of 0.5 mg/cm 2 ) was formed on the surface of the HRL layer of the separator sheet. Then, a battery of Example 3 was produced in the same manner as in Example 1 except that a separator sheet including the PEO layer was used in place of the PEO sheet and the separator sheet.
  • a wound electrode body of the battery of Example 3 had a configuration shown in FIG. 5 .
  • Comparative Examples 2 and 3 the PE or PP sheet was interposed between the negative electrode sheet and the separator sheet, and thus the space between positive and negative electrodes was larger than in Comparative Example 1, and the limit current value was also smaller than in Comparative Example 1. In other words, Li precipitation resistance decreased.
  • Comparative Example 4 the space between positive and negative electrodes was slightly larger and Li precipitation resistance was slightly greater than in Comparative Example 1, but wrinkles were still observed in the separator.

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